JP2006508958A5 - - Google Patents

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JP2006508958A5
JP2006508958A5 JP2004551161A JP2004551161A JP2006508958A5 JP 2006508958 A5 JP2006508958 A5 JP 2006508958A5 JP 2004551161 A JP2004551161 A JP 2004551161A JP 2004551161 A JP2004551161 A JP 2004551161A JP 2006508958 A5 JP2006508958 A5 JP 2006508958A5
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Japan
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acid
composition according
pharmaceutical composition
anticancer agent
carnitine
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JP2004551161A
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Japanese (ja)
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JP2006508958A (en
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Priority claimed from US10/292,823 external-priority patent/US20030199535A1/en
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Claims (27)

末梢神経障害誘発性抗癌剤、但し該抗癌剤はタキソールやシスプラチンではない、の投与によって誘発される末梢神経障害を予防および/または処置するための、アセチルL-カルニチンまたはその薬学的に許容し得る塩を含有する医薬組成物。 Peripheral neuropathy induced anticancer proviso that the anticancer agent is not taxol or cisplatin, for the prevention and / or treatment of peripheral neuropathy induced by administration of acetyl L- carnitine or a pharmaceutically acceptable salt thereof A pharmaceutical composition containing. 該医薬品が協調的方法による投与に適当である、請求項1記載の医薬組成物2. A pharmaceutical composition according to claim 1 wherein the medicament is suitable for administration in a coordinated manner. 該末梢神経障害誘発性抗癌剤が、プラチン化合物ファミリー、タキサン、エポシロン類およびビンカアルカロイド、ファルネシル転移酵素阻害剤、サリドマイド、5-フルオロウラシル、クリプトフィジンアナログ、プロテアソーム阻害剤から選択される、請求項1または2記載の医薬組成物Or 2. The pharmaceutical composition according to 2 . 該抗癌剤が、カルボプラチン、オキサリプラチン、ドセタキセル、エポシロン、ビノレルビン、ビンクリスチン、ファルネシル転移酵素阻害剤R11577、サリドマイド、クリプトフィジンアナログLY355703、プロテアソーム阻害剤PS341からなる群から選択される、請求項3記載の医薬組成物 The medicament according to claim 3, wherein the anticancer agent is selected from the group consisting of carboplatin, oxaliplatin, docetaxel, epothilone, vinorelbine, vincristine, farnesyltransferase inhibitor R11577, thalidomide, cryptophysin analog LY355703, and proteasome inhibitor PS341. Composition . 該投与が実質的に同時である、請求項2〜4のいずれかに記載の医薬組成物 The pharmaceutical composition according to any of claims 2 to 4, wherein the administration is substantially simultaneous. 該投与が逐次的である、請求項2〜4のいずれかに記載の医薬組成物 The pharmaceutical composition according to any of claims 2 to 4, wherein the administration is sequential. 該投与が、該アセチルL-カルニチンまたはその薬学的に許容し得る塩を、抗癌剤、さらに所望により薬学的に許容し得る賦形剤および/またはビヒクルとの組合せを混合物として含む組成物の形態にある、請求項2〜5のいずれかに記載の医薬組成物The administration is in the form of a composition comprising a combination of the acetyl L-carnitine or a pharmaceutically acceptable salt thereof in combination with an anti-cancer agent, and optionally a pharmaceutically acceptable excipient and / or vehicle. The pharmaceutical composition according to any one of claims 2 to 5. 0.1〜3g/日のアセチルL-カルニチンまたは等量のその薬学的に許容し得る塩が投与される、請求項1〜7のいずれかに記載の医薬組成物 The pharmaceutical composition according to any of claims 1 to 7, wherein 0.1 to 3 g / day of acetyl L-carnitine or an equivalent amount of a pharmaceutically acceptable salt thereof is administered. 該アセチルL-カルニチンの薬理学的に許容し得る塩が、塩化物、臭化物、オロチン酸塩、酸アスパラギン酸塩、酸クエン酸塩、酸リン酸塩、フマル酸および酸フマル酸、マレイン酸塩および酸マレイン酸、酸シュウ酸塩、酸硫酸塩、グルコースリン酸塩、酒石酸塩および酸酒石酸塩からなる群から選択される、請求項1〜8のいずれかに記載の医薬組成物The pharmacologically acceptable salts of acetyl L-carnitine are chloride, bromide, orotate, acid aspartate, acid citrate, acid phosphate, fumaric acid and acid fumaric acid, maleate And a pharmaceutical composition according to any of claims 1 to 8, selected from the group consisting of acid maleic acid, acid oxalate, acid sulfate, glucose phosphate, tartrate and acid tartrate. 該医薬品が、該抗癌剤による処置が必要と考えられる被検者に投与されるものである、請求項1〜4および6〜9のいずれかに記載の医薬組成物 The pharmaceutical composition according to any one of claims 1 to 4 and 6 to 9, wherein the medicament is administered to a subject who is considered to require treatment with the anticancer agent. 該医薬品が、腫瘍の外科的除去の直前または直後に投与されるものである、請求項10記載の医薬組成物 The pharmaceutical composition according to claim 10, wherein the pharmaceutical is administered immediately before or after the surgical removal of the tumor. 該抗癌剤が腫瘍の外科的除去に代わるものである、請求項10記載の医薬組成物11. The pharmaceutical composition according to claim 10, wherein the anticancer agent is an alternative to surgical removal of the tumor. 別のカルニチンまたはその薬学的に許容し得る塩が添加される、請求項1〜12のいずれかに記載の医薬組成物 The pharmaceutical composition according to any one of claims 1 to 12, wherein another carnitine or a pharmaceutically acceptable salt thereof is added. さらなる抗癌剤が添加される、請求項1〜13のいずれか記載の医薬組成物 The pharmaceutical composition according to any one of claims 1 to 13, wherein an additional anticancer agent is added. a)アセチルL-カルニチンまたはその薬学的に許容し得る塩、
b)末梢神経障害誘発性抗癌剤
を組み合わせて含む、組成物。
a) Acetyl L-carnitine or a pharmaceutically acceptable salt thereof,
b) A composition comprising a combination of peripheral neuropathy-inducing anticancer agents.
該抗癌剤が、プラチン化合物ファミリーの群、タキサン、エポシロン類、ビンカアルカロイドから選択される、請求項15記載の組成物。 16. The composition of claim 15, wherein the anticancer agent is selected from the group of platin compound families, taxanes, epothilones, vinca alkaloids. 該抗癌剤が、プラチン化合物、タキサン、エポシロン類およびビンカアルカロイド、ファルネシル転移酵素阻害剤、サリドマイド、5-フルオロウラシル、クリプトフィジンアナログ、プロテアソーム阻害剤からなる群から選択される、請求項16記載の組成物。 The composition according to claim 16, wherein the anticancer agent is selected from the group consisting of a platin compound, a taxane, an epothilone and a vinca alkaloid, a farnesyltransferase inhibitor, a thalidomide, 5-fluorouracil, a cryptophysin analog, and a proteasome inhibitor. . 該抗癌剤が、カルボプラチン、オキサリプラチン、ドセタキセル、エポシロン、ビノレルビン、ビンクリスチン、ファルネシル転移酵素阻害剤R11577、サリドマイド、クリプトフィジンアナログLY355703、プロテアソーム阻害剤PS341からなる群から選択される、請求項17記載の組成物。 The composition according to claim 17, wherein the anticancer agent is selected from the group consisting of carboplatin, oxaliplatin, docetaxel, epothilone, vinorelbine, vincristine, farnesyltransferase inhibitor R11577, thalidomide, cryptophysin analog LY355703, and proteasome inhibitor PS341. object. アセチルL-カルニチンの薬理学的に許容し得る塩が、塩化物、臭化物、オロチン酸塩、酸アスパラギン酸塩、酸クエン酸塩、酸リン酸塩、フマル酸塩および酸フマル酸塩、マレイン酸塩および酸マレイン酸塩、酸シュウ酸塩、酸硫酸塩、グルコースリン酸塩、酒石酸塩および酸酒石酸塩からなる群から選択される、請求項15〜18のいずれかに記載の組成物。 The pharmacologically acceptable salts of acetyl L-carnitine are chloride, bromide, orotate, acid aspartate, acid citrate, acid phosphate, fumarate and acid fumarate, maleic acid 19. A composition according to any of claims 15-18, selected from the group consisting of salts and acid maleates, acid oxalates, acid sulfates, glucose phosphates, tartrate and acid tartrate. 別のカルニチンまたはその薬学的に許容し得る塩が添加される、請求項15〜19のいずれかに記載の組成物。 20. A composition according to any of claims 15 to 19, wherein another carnitine or a pharmaceutically acceptable salt thereof is added. 別の抗癌剤が添加される、請求項15〜20のいずれかに記載の組成物。 21. A composition according to any of claims 15-20, wherein another anticancer agent is added. a)治療上有効量の末梢神経障害誘発性抗癌剤を含む医薬組成物、
b)該抗癌剤の投与によって誘発された末梢神経障害に対して実質的な保護作用を生ずるのに適切な量で、アセチルL-カルニチンまたはその薬学的に許容し得る塩を含む医薬組成物を含む、
キット。
a) a pharmaceutical composition comprising a therapeutically effective amount of a peripheral neuropathy-inducing anticancer agent;
b) comprising a pharmaceutical composition comprising acetyl L-carnitine or a pharmaceutically acceptable salt thereof in an amount suitable to produce a substantial protective effect against peripheral neuropathy induced by administration of said anticancer agent. ,
kit.
該抗癌剤が、プラチン化合物群、タキサン、エポシロン類およびビンカアルカロイド、ファルネシル転移酵素阻害剤、サリドマイド、5-フルオロウラシル、クリプトフィジンアナログ、プロテアソーム阻害剤から選択される、請求項22記載のキット。 The kit according to claim 22, wherein the anticancer agent is selected from the group of platin compounds, taxanes, epothilones and vinca alkaloids, farnesyltransferase inhibitors, thalidomide, 5-fluorouracil, cryptophysin analogs, proteasome inhibitors. 該抗癌剤が、カルボプラチン、オキサリプラチン、ドセタキセル、エポシロン、ビノレルビン、ビンクリスチン、ファルネシル転移酵素阻害剤R11577、サリドマイド、クリプトフィジンアナログLY355703、プロテアソーム阻害剤PS341からなる群から選択される、請求項23記載のキット。 The kit according to claim 23, wherein the anticancer agent is selected from the group consisting of carboplatin, oxaliplatin, docetaxel, epothilone, vinorelbine, vincristine, farnesyltransferase inhibitor R11577, thalidomide, cryptophysin analog LY355703, and proteasome inhibitor PS341. . アセチルL-カルニチンの薬理学的に許容し得る塩が、塩化物、臭化物、オロチン酸塩、酸アスパラギン酸塩、酸クエン酸塩、酸リン酸塩、フマル酸塩および酸フマル酸塩、マレイン酸塩および酸マレイン酸、酸シュウ酸塩、酸硫酸塩、グルコースリン酸塩、酒石酸塩および酸酒石酸塩からなる群から選択される、請求項22〜24のいずれかに記載のキット。 Pharmacologically acceptable salts of acetyl L-carnitine are chloride, bromide, orotate, acid aspartate, acid citrate, acid phosphate, fumarate and acid fumarate, maleic acid 25. Kit according to any of claims 22 to 24, selected from the group consisting of salts and acid maleic acid, acid oxalate, acid sulfate, glucose phosphate, tartrate and acid tartrate. さらなるカルニチンまたはその薬学的に許容し得る塩が添加される、請求項22〜25のいずれかに記載のキット。 26. Kit according to any of claims 22 to 25, wherein additional carnitine or a pharmaceutically acceptable salt thereof is added. さらなる抗癌剤が添加される、請求項22〜26のいずれかに記載の組成物。 27. A composition according to any of claims 22 to 26, wherein an additional anticancer agent is added.
JP2004551161A 2002-11-13 2003-10-23 Pharmaceuticals for preventing and / or treating peripheral neuropathy induced by anticancer agents Pending JP2006508958A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/292,823 US20030199535A1 (en) 1998-07-30 2002-11-13 Method for preventing and/or treating peripheral neuropathies induced by the administration of an anticancer agent
PCT/IT2003/000656 WO2004043454A1 (en) 2002-11-13 2003-10-23 Acetyl-l-carnitine for the prevention and/or treatment of peripheral neuropathies induced by anticancer agents

Publications (2)

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JP2006508958A JP2006508958A (en) 2006-03-16
JP2006508958A5 true JP2006508958A5 (en) 2006-11-30

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US (2) US20030199535A1 (en)
EP (1) EP1562577B1 (en)
JP (1) JP2006508958A (en)
KR (1) KR20050075012A (en)
CN (1) CN1708297A (en)
AR (1) AR041947A1 (en)
AT (1) ATE526958T1 (en)
AU (2) AU2003283807B2 (en)
BR (1) BR0316131A (en)
CA (1) CA2505937C (en)
CY (1) CY1112399T1 (en)
DK (1) DK1562577T3 (en)
ES (1) ES2374503T3 (en)
MX (1) MXPA05004752A (en)
PL (1) PL379244A1 (en)
PT (1) PT1562577E (en)
SI (1) SI1562577T1 (en)
TW (1) TWI362260B (en)
WO (1) WO2004043454A1 (en)

Families Citing this family (11)

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Publication number Priority date Publication date Assignee Title
AU2002313817A1 (en) * 2001-08-27 2003-03-10 Advanced Cell Technology, Inc. Trans-differentiation and re-differentiation of somatic cells and production of cells for cell therapies
WO2004018478A2 (en) 2002-08-23 2004-03-04 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto, analogues and uses thereof
US7649006B2 (en) 2002-08-23 2010-01-19 Sloan-Kettering Institute For Cancer Research Synthesis of epothilones, intermediates thereto and analogues thereof
ITMI20070817A1 (en) * 2007-04-19 2008-10-20 Farmacetika Ltd PHARMACEUTICAL COMPOSITION INCLUDING L-CARNITINE AND AN ANTAGONIST AGENT OF MEMBRANE ADENOSIN RECEPTORS, THEIR DERIVATIVES AND / OR PHARMACEUTICALLY ACCEPTABLE SALTS, AND USE OF THE SAME IN THE PREPARATION OF DRUGS WITH NON-TOXIC EFFECT OF INIBI
JP4208036B1 (en) * 2007-04-26 2009-01-14 日本新薬株式会社 Pharmaceutical composition for inhibiting peripheral neuropathy associated with administration of anticancer agents
CA2698129A1 (en) * 2007-08-31 2009-03-05 Kyushu University, National University Corporation Prophylactic or alleviating agent for peripheral nerve disorder induced by anti-cancer agent
RU2485956C2 (en) * 2007-10-30 2013-06-27 Трофо New composition for treating side effects of anti-cancer therapy
CA2740347A1 (en) * 2008-12-01 2010-06-10 Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. Use of alkanoyl l-carnitine in combination with chemotherapeutic agents for the treatment of neoplasms
CN102060722B (en) * 2009-05-01 2014-06-11 常州高新技术产业开发区三维工业技术研究所有限公司 Arsenic compound and preparation method and use thereof
ITPZ20130005A1 (en) * 2013-07-05 2015-01-06 Teodosio Antonio Ferrara ENERGETIC METABOLISM AND HOMEOSTASIS
EP3538093B1 (en) 2016-11-09 2023-10-25 Qiagen Sciences, LLC Photoprotective mixtures as imaging reagents in sequencing-by-synthesis

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* Cited by examiner, † Cited by third party
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US4713370A (en) * 1972-11-06 1987-12-15 Felice Stephen L De Carnitine and its use in reducing cardiac toxicity and as a synergist with cytostats
US4599352A (en) * 1984-03-01 1986-07-08 The United States Of America As Represented By The Department Of Health And Human Services Antineoplastic platinum (IV) complexes and compositions
IT1196564B (en) * 1986-08-04 1988-11-16 Sigma Tau Ind Farmaceuti USE OF ACETYL L-CARNITINE IN THE THERAPEUTIC TREATMENT OF PERIPHERAL NEUROPATHIES
JP4703851B2 (en) * 1998-07-30 2011-06-15 シグマ−タウ・インドゥストリエ・ファルマチェウチケ・リウニテ・ソシエタ・ペル・アチオニ Use of L-carnitine and its alkanoyl derivative for the manufacture of a medicament having anticancer activity

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